The synthesis of 1,4-diazacycl[3,2,2]azine

The diazaanalog of “cycl[3,2,2]azine”, “1,4-diazacycl[3,2,2]azine” (1,4,7b-triazacyclopent-[cd]indene) and its 2-methyl derivative were prepared. These compounds are subject to facile acid-catalyzed hydrolysis affording substituted imidazo[1,2-a]pyridines.     

Preparation of 2,4-diarylquinolines and substituted dihydrobenz-[c]acridines by the condensation of certain c(α),o-dilithiooximes with 2-aminobenzophenones

C(α),O-Dilithiooximes were prepared in an excess of lithium diisopropylamide and condensed with several 2-aminobenzophenones, followed by acid hydrolysis of the oximes to the ketones, which then underwent cyclodehydration and linear dehydration to give substituted quinolines or dihydrobenz[c]acridines.     

Characterization of the short-chain branches in poly(vinyl chloride)s by γ irradiation of the reduced polymers

The volatile products from the γ irradiation of samples of poly(vinyl chloride) prepared under different conditions and reduced to the corresponding polyethylenes have been measured quantitatively and compared with those for low- and high-density polyethylenes and copolymers of ethylene with small amounts of α-olefins. The presence of methyl branches is clearly demonstrated and there is also evidence for ethyl and butyl branches, although these had not been considered significant in previous [¹³C] NMR studies. The method is shown to be extremely sensitive to small quantities of residual trialkyl tin hydride reductant occluded in, and possibly also reacted with, the polymer, and to residual chlorine (<0.5%). The yields of alkanes are higher than expected from the branch frequencies determined by i.r. and [¹³C] NMR and results for ethylene-α-olefin copolymers. This difference is apparently due to sensitisation of the radiation degradation by residual chlorine and reductant. Quantitative determinations of branch frequencies by the radiolytic method are unlikely to be obtained until these problems are overcome.     

Reaction of γ-picoline N-oxide with ketenimines in the presence of organic acids: Preparation of α-acyloxyamides

A synthesis of a-acyloxyamides is described which utilizes the reaction of 7-picoline N-oxide and various organic acids with diphenylketene N-p-tolylimine.